Strategy to develop broadly effective multivalent COVID-19 vaccines against emerging variants based on Ad5/35 platform
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron strain has evolved into highly divergent variants with several sub-lineages. These newly emerging variants threaten the efficacy of available COVID-19 vaccines. To mitigate the occurrence of breakthrough infections and re-infections, and more importantly, to reduce the disease burden, it is essential to develop a strategy for producing updated multivalent vaccines that can provide broad neutralization against both currently circulating and emerging variants. We developed bivalent vaccine AdCLD-CoV19-1 BA.5/BA.2.75 and trivalent vaccines AdCLD-CoV19-1 XBB/BN.1/BQ.1.1 and AdCLD-CoV19-1 XBB.1.5/BN.1/BQ.1.1 using an Ad5/35 platform-based non-replicating recombinant adenoviral vector. We compared immune responses elicited by the monovalent and multivalent vaccines in mice and macaques. We found that the BA.5/BA.2.75 bivalent and the XBB/BN.1/BQ.1.1 and XBB.1.5/BN.1/BQ.1.1 trivalent vaccines exhibited improved cross-neutralization ability compared to their respective monovalent vaccines. These data suggest that the developed multivalent vaccines enhance immunity against circulating Omicron subvariants and effectively elicit neutralizing antibodies across a broad spectrum of SARS-CoV-2 variants.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:121 |
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Enthalten in: |
Proceedings of the National Academy of Sciences of the United States of America - 121(2024), 10 vom: 05. März, Seite e2313681121 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Chang, Soojeong [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 28.02.2024 Date Revised 14.03.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1073/pnas.2313681121 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM368981959 |
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520 | |a The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron strain has evolved into highly divergent variants with several sub-lineages. These newly emerging variants threaten the efficacy of available COVID-19 vaccines. To mitigate the occurrence of breakthrough infections and re-infections, and more importantly, to reduce the disease burden, it is essential to develop a strategy for producing updated multivalent vaccines that can provide broad neutralization against both currently circulating and emerging variants. We developed bivalent vaccine AdCLD-CoV19-1 BA.5/BA.2.75 and trivalent vaccines AdCLD-CoV19-1 XBB/BN.1/BQ.1.1 and AdCLD-CoV19-1 XBB.1.5/BN.1/BQ.1.1 using an Ad5/35 platform-based non-replicating recombinant adenoviral vector. We compared immune responses elicited by the monovalent and multivalent vaccines in mice and macaques. We found that the BA.5/BA.2.75 bivalent and the XBB/BN.1/BQ.1.1 and XBB.1.5/BN.1/BQ.1.1 trivalent vaccines exhibited improved cross-neutralization ability compared to their respective monovalent vaccines. These data suggest that the developed multivalent vaccines enhance immunity against circulating Omicron subvariants and effectively elicit neutralizing antibodies across a broad spectrum of SARS-CoV-2 variants | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Shin, Kwang-Soo |e verfasserin |4 aut | |
700 | 1 | |a Park, Bongju |e verfasserin |4 aut | |
700 | 1 | |a Park, Seowoo |e verfasserin |4 aut | |
700 | 1 | |a Shin, Jieun |e verfasserin |4 aut | |
700 | 1 | |a Park, Hyemin |e verfasserin |4 aut | |
700 | 1 | |a Jung, In Kyung |e verfasserin |4 aut | |
700 | 1 | |a Kim, Jong Heon |e verfasserin |4 aut | |
700 | 1 | |a Bae, Seong Eun |e verfasserin |4 aut | |
700 | 1 | |a Kim, Jae-Ouk |e verfasserin |4 aut | |
700 | 1 | |a Baek, Seung Ho |e verfasserin |4 aut | |
700 | 1 | |a Kim, Green |e verfasserin |4 aut | |
700 | 1 | |a Hong, Jung Joo |e verfasserin |4 aut | |
700 | 1 | |a Seo, Hyungseok |e verfasserin |4 aut | |
700 | 1 | |a Volz, Erik |e verfasserin |4 aut | |
700 | 1 | |a Kang, Chang-Yuil |e verfasserin |4 aut | |
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